CQV Professional – Lab and Facilities

vor 20 Stunden

Stein, Schweiz Coopers Group AG Vollzeit
CQV Professional – Lab and Facilities (CDMO)

Are you a seasoned professional with extensive technical expertise in CQV? We are looking for CQV Engineers to join our client's team in Visp and Stein on a contract basis. The roles require a deep understanding of Qualification, Commissioning, and verification of both lab equipment and facilities.

Key Responsibilities:

  • Lead and execute commissioning, qualification, and validation (CQV) activities for laboratory equipment, cleanrooms, and critical facility systems (e.g., HVAC, utilities, and water systems).
  • Develop, review, and approve validation protocols, reports, and documentation to ensure compliance with regulatory standards and industry best practices.
  • Troubleshoot and resolve CQV-related issues, collaborating with engineering, quality, and operations teams to drive project success.

Must Haves:

  • Bachelor’s degree in Engineering, Life Sciences, or related field with 3+ years of experience in CQV for laboratory and facility systems.
  • Strong knowledge of regulatory requirements (e.g., cGMP, ICH Q9, Q10) and validation lifecycle for pharmaceutical/biotech facilities.
  • Proven ability to manage multiple projects simultaneously with excellent communication and problem-solving skills.

If you’re passionate about delivering high-quality solutions and thrive in a fast-paced CDMO environment, we invite you to apply and make an impact

Seniority level
  • Mid-Senior level
Employment type
  • Contract
Job function
  • Science and Engineering
  • Industries: Pharmaceutical Manufacturing
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